Last synced on 25 January 2026 at 3:41 am

b-ONE MOBIO Total Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213673
510(k) Type
Traditional
Applicant
B-One Ortho, Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2022
Days to Decision
60 days
Submission Type
Summary

b-ONE MOBIO Total Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213673
510(k) Type
Traditional
Applicant
B-One Ortho, Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2022
Days to Decision
60 days
Submission Type
Summary